tag:www.gov.uk,2005:/search/guidance-and-regulation Guidance and regulation 2025-06-13T16:26:39+01:00 HM 바카라 사이트 tag:www.gov.uk,2005:/government/publications/medicines-eligible-for-northern-ireland-mhra-authorised-route 2025-06-13T16:26:39+01:00 Medicines eligible for Northern Ireland MHRA Authorised Route Sets out medicines that can be moved to Northern Ireland to meet patient need. tag:www.gov.uk,2005:/government/publications/medicines-that-cannot-be-parallel-exported-from-the-uk 2025-06-10T17:08:52+01:00 Medicines that you cannot export from the UK or hoard Sets out medicines that cannot be exported from the UK or hoarded because they are needed for UK patients. tag:www.gov.uk,2005:/government/publications/human-medicines-modular-manufacture-and-point-of-care-regulations-2025-overview 2025-06-10T13:57:05+01:00 Human medicines Modular Manufacture and Point of Care regulations 2025: Overview Helping interpret the Human Medicines (Amendment) Modular Manufacture and Point of Care regulations 2025. tag:www.gov.uk,2005:/guidance/supplying-authorised-medicines-to-northern-ireland 2025-06-09T11:21:39+01:00 Supplying authorised medicines to Northern Ireland What you need to do to supply authorised medicines from Great Britain to Northern Ireland. tag:www.gov.uk,2005:/government/publications/disapplication-of-falsified-medicines-directive-safety-features-requirements-for-parallel-imports 2025-06-03T14:54:12+01:00 Disapplication of Falsified Medicines Directive Safety Features: Requirements for Parallel Imports Information relating to the disapplication of falsified medicines under UK Law. tag:www.gov.uk,2005:/government/publications/uk-parallel-import-licences-following-agreement-of-the-windsor-framework 2025-06-03T14:52:44+01:00 UK parallel import licences following agreement of the Windsor Framework Information relating to parallel imports and the implementation of the Windsor Framework. tag:www.gov.uk,2005:/government/publications/medical-devices-uk-approved-bodies 2025-05-23T19:10:20+01:00 Medical devices: list of UK approved bodies Details of the organisations that are currently approved to undertake conformity assessments on medical devices. tag:www.gov.uk,2005:/guidance/medicines-reclassify-your-product 2025-05-16T12:17:18+01:00 Medicines: reclassify your product Pharmacy (P), prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification. tag:www.gov.uk,2005:/government/publications/the-northern-ireland-mhra-authorised-route-nimar 2025-05-09T11:14:01+01:00 The Northern Ireland MHRA Authorised Route (NIMAR) The UK government has introduced the Northern Ireland MHRA Authorised Route (NIMAR). This new route for supply became operational 1 January 2022. tag:www.gov.uk,2005:/guidance/export-drugs-and-medicines-special-rules 2025-04-01T09:13:43+01:00 Export drugs and medicines: special rules You must get permission to export certain drugs and medicines. tag:www.gov.uk,2005:/guidance/medicines-register-to-manufacture-import-or-distributor-active-substances 2025-04-01T09:13:28+01:00 Medicines: register to manufacture, import or distribute active substances How to register as a manufacturer, importer or distributor of active substances. tag:www.gov.uk,2005:/guidance/medicines-register-as-a-broker 2025-04-01T09:13:20+01:00 Medicines: register as a broker Apply for and maintain registrations for the brokering of human medicines. tag:www.gov.uk,2005:/government/publications/wholesalers-manufacturers-guidance-following-agreement-of-the-windsor-framework 2025-03-11T10:03:49+00:00 Wholesalers & manufacturers guidance following agreement of the Windsor Framework Actions QPs, RPis and RPs need to take following agreement of the Windsor Framework tag:www.gov.uk,2005:/government/publications/importing-investigational-medicinal-products-into-great-britain-from-approved-countries 2025-02-12T15:51:21+00:00 Importing investigational medicinal products into Great Britain from approved countries Outlining the principles for the management and oversight of the import of investigational medicinal products (IMPs) to Great Britain from listed countries. tag:www.gov.uk,2005:/guidance/import-a-human-medicine 2025-01-29T09:01:44+00:00 Import a human medicine Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs. tag:www.gov.uk,2005:/guidance/guidance-on-mah-and-qppv-location 2025-01-08T16:31:09+00:00 Guidance on MAH and QPPV location The locations for a Marketing Authorisation Holder (MAH) and a Qualified Person responsible for Pharmacovigilance (QPPV) tag:www.gov.uk,2005:/government/publications/exporting-active-substances-manufactured-in-great-britain-for-use-in-eea-and-northern-ireland 2025-01-02T15:26:24+00:00 Exporting active substances manufactured in Great Britain for use in EEA and Northern Ireland How the 바카라 사이트˜Written Confirmation바카라 사이트™ process operates for active substances manufactured in Great Britain (England, Wales and Scotland). tag:www.gov.uk,2005:/guidance/sourcing-medicines-for-the-great-britain-market-from-an-approved-country-for-import-or-northern-ireland 2024-12-30T16:48:56+00:00 Sourcing medicines for the UK market Information on sourcing medicines that can be supplied by wholesale distributor authorisation (WDA) holders based in the UK. tag:www.gov.uk,2005:/government/publications/uk-medicines-export-and-labelling-for-international-regulators 2024-12-30T00:00:00+00:00 UK medicines export and Windsor Framework labelling requirements Supplementary information for international regulators on packaging changes and the export of UK medicines. tag:www.gov.uk,2005:/government/publications/windsor-framework-webinar-recordings 2024-11-14T12:44:10+00:00 Windsor Framework Webinar Recordings A series of webinars providing guidance on the Windsor Framework agreement and the supply of medicines in Northern Ireland.